A clinical case of autosomal recessive agammaglobulinemia with B-cell deficiency
Background. Primary agammaglobulinemia is the result of specific changes in B-cells that lead to low antibody production. A preliminary diagnosis is established if there is a history of frequent bacterial infections (otitis media, sinusitis, skin abscesses), including severe course, in some cases ca...
Saved in:
Main Authors: | E. V. Negodnova, M. S. Iskandyarova, E. N. Tyagusheva, O. A. Radaeva, G. V. Fominova |
---|---|
Format: | Article |
Language: | Russian |
Published: |
Association of Paediatric Allergists and Immunologists of Russia (APAIR)
2024-01-01
|
Series: | Аллергология и Иммунология в Педиатрии |
Subjects: | |
Online Access: | https://adair.elpub.ru/jour/article/view/120 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
by: Ying Xie, et al.
Published: (2025-07-01) -
Multimorbid Patient with Primary Immunodeficiency. Diagnostics, Treatment
by: V. N. Larina, et al.
Published: (2025-03-01) -
Coexistence of Griscelli Syndrome Type 2 and Autosomal Recessive Congenital Ichthyosis in an Indian Girl
by: Yashika Jayesh Doshi, et al.
Published: (2025-04-01) -
Clinical case of primary immunodeficiency: X-linked agammaglobulinemia
by: E. V. Kuvschinova, et al.
Published: (2020-04-01) -
Prenatal Ultrasound Diagnostics of Autosomal Recessive Polycystic Kidney Disease in Fetus: Clinical Case
by: Nodira M. Normuradova, et al.
Published: (2022-05-01)